Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/1732
Full metadata record
DC FieldValueLanguage
dc.contributor.authorKumar, P. Vijaya-
dc.contributor.authorReddy, K. Manoher-
dc.contributor.authorRao, V. Rajeswar-
dc.date.accessioned2024-11-25T06:37:29Z-
dc.date.available2024-11-25T06:37:29Z-
dc.date.issued2008-
dc.identifier.urihttp://localhost:8080/xmlui/handle/123456789/1732-
dc.descriptionNITWen_US
dc.description.abstractReaction of 3-(2-amino-4-thiazolyl)coumarins with ethyl acetoacetate in a mixture of PPA and POCl3 give 7-methyl-3 (2-oxo-2H-chromen-3-yl)-5H-thiazolo[3,2-a]pyrimidin-5-ones in a single step. Alternatively condensation of 3-(2-amino-4 thiazolyl)coumarins 1 with acetoacetic ester (EAA) 2 results in the formation of Schiff bases 3a-g. These on further reaction with polyphosphoric acid (PPA) and phosphorus oxychloride (POCl3) give corresponding cyclised compounds. 7-methyl-3(2-oxo-2H-chromen-3-yl)-5H[1,3]thiazolo[3,2-a]pyrimidin-5-ones 4a-g. The structures of newly prepared compounds have been confirmed from analytical and spectral data.en_US
dc.language.isoenen_US
dc.publisherIndian Journal of Chemistry - Section B Organic and Medicinal Chemistryen_US
dc.subjectBenzopyran-2-oneen_US
dc.subjectPyrimidin-5-onesen_US
dc.subjectThiazolesen_US
dc.subjectThiazolo pyrimidonesen_US
dc.titleSynthesis of some 7-methyl-3-(2-oxo-2H-chromen-3-yl)-5H[1,3]thiazolo[3,2-a] -pyrimidin-5-onesen_US
dc.typeArticleen_US
Appears in Collections:Chemistry

Files in This Item:
File Description SizeFormat 
A new withanolide from the roots of Withania somnifera.pdf58.72 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.